| Joined: Aug 2009 Posts: 38 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Aug 2009 Posts: 38 | David, I understand your point and appreciate any information you can offer other than that it does not make sense. I am giving you all of the info that I am getting and please keep in mind that I am here because I have the same frustration that you do. It does not help me to be reprimanded for not being able to make my information make sense. I am just looking for an outlet and, unfortunately, right now this is the only one that I have. I keep hoping that something that I post will make all of the pieces fit. Sorry that it annoys you.
Charm, Thank you SO much for this positive post. I have printed this out and have a feeling that it will somehow land in his truck seat. I strongly feel that he is being unfair, but my telling them would cause him to withdraw from me and I cannot loose what little time I have left with him. Selfish, yes. But I also have to weigh in on the fact that he thinks this will send his dad over the edge with his stroke recovery and blood pressure already in bad shape. If I were to tell them and Brian lost his dad because he had another stoke, where does that leave my decision? I think it definately has to be his decision to talk. Thanks for this wonderful article though. Teresa
CG SCC of lower gum. DX 6/09, SURGERY 7/09, MTX Started 8/09. Single RX treatment 8/18/09
| | | | Joined: May 2008 Posts: 551 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: May 2008 Posts: 551 | Teresa,
Do you have a relationship with Brian's family? Have you considered what will happen after he's gone and they realize you knew what was happening and didn't give them the chance to help and support their son and brother?
I don't think I could support someone in that decision as you are doing. Brian is making an impossible situation even more difficult, and quite frankly, I think the way he's treating you is downright cruel.
Stage IV SCC lt lateral tongue, surgery 5/19/08 (partial gloss/upper neck dissection left side/radial free flap reconstruction) IMRT w/weekly Cisplatin & Erbitux 6/30/08, PEG 1 6/12/08 - out 7/14 (in abdominal wall, not stomach), PEG 2 7/23/08 - out 11/20/08, Tx done 8/18/08 Second SCC tumor, Stage 1, rt mobile tongue, removed 10/18/2016, right neck dissection 12/9/2016 Third SCC tumor, diagnosed, 4/19/2108, rt submandibular mass, HPV-, IMRT w/ weekly Cisplatin, 5/9 - 6/25/2018, PEG 3 5/31/2018
| | | | Joined: Jan 2009 Posts: 476 Platinum Member (300+ posts) | Platinum Member (300+ posts) Joined: Jan 2009 Posts: 476 | Teresa, I was away and just read this entire post. First I am so, so sorry you are going through this and quite frankly I don't know how you are dealing with all this. If you read my signature you can read all my husband has been through. When my husband was diagnosed he had never been sick a day in his life, never smoked, ate right, took vitamins every day and still got slammed with this. As a caregiver the past 8 months have been some of the most difficult and yet some of the most loved-filled months of my life. My husband is also a very private person and didn't want people knowing he was sick and couldn't even say the word "cancer". He would refer to it as his "condition" or "situation". Our doctors basically told us that chemo alone does nothing for this type of cancer. Chemo would help enhance the radiation and that is what we went for - total cure. My husband told me from day one that he would give it his best shot and go for the treatment all his doctors agreed on. Thank God we are now on the other side but we don't relax totally thinking that it couldn't come back. My husband already told me that if the cancer comes back he won't seek further treatments. That scares me to death knowing how many people on the boards who have had treatment and had recurrances.
In the beginning my husband would get very angry when I would discuss his "situation" with people but I wear my heart on my sleeve and could have never survived this without support from my family, friends and co-workers. When John was deep in the middle of treatments and could no longer talk, he would leave me the most loving notes telling me I was his rock and he could never get through this without me. To me - that's love. John told me during treatments that he wanted to stop because it was just to difficult but couldn't bear the thought of me being left alone without him or leaving his 83 year old mom alone. I think it is totally selfish of your boyfriend to not let his family know what is going on and I think they will be very angry if he dies from this and they find out that you knew.
I don't think your boyfriend is in denial I think he obviously has a strong self-destructive streak and doesn't care enough about his loved ones to share this. I really wish there was something I could say to make you feel better. The reality is that this WILL kill him. With the treatment (if you want to call it that) he is currently doing I would be surprised if he survived months or weeks. I to believe in prayer and miracles. But if prayers alone worked, I wouldn't have watched my mom die from pancreatic cancer after a 3 1/2 year battle and she was caught early. I will continue to pray for you to give you the strength to do what is right for you. Wanda
Wanda (47) caregiver to husband John (56) age at diag.(2009) 1-13-09 diagnosed Stage IV BOT SCC (HPV+) 2-12-09 PEG placed, 7-6-09 removed Cisplatin 7 weeks, 7 weeks (35) IMRT 4-15-09 - treatment completed 8-09,12-09-CT Scans clear, 4-10,6-11-PET Scans clear 4-2013 - HBO (30 dives) tooth extraction 10-2019 - tooth extraction, HBO (10 dives) 11-2019 - Left lateral tongue SCC - Stage 2
| | | | Joined: Feb 2007 Posts: 1,940 "OCF across the pond" Patient Advocate (1000+ posts) | "OCF across the pond" Patient Advocate (1000+ posts) Joined: Feb 2007 Posts: 1,940 | I have to say i am 100% behind David on this one.Absolutely nothing that he has told you is recognisable as treatment or symptoms of Oral Cancer.It just doesn't make any sense at all.Thats not your fault and must be equally frustrating for you as it is for us,as it is almost impossible to give help and advice.I am at a loss,and really have no idea how to offer anything that will be of help to you.
Liz in the UK
Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007 Recurrence June/07 died July 29th/07.
Never take your eye off the ball, it may just smack you in the mouth.
| | | | Joined: Dec 2008 Posts: 1,004 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Dec 2008 Posts: 1,004 | Teresa,
Have you gone to any appointment with him yet? Is it a possibilty that he is not telling you the truth?
Suzanne *********** T1 SCC on right side of tongue Age 31...27 when diagnosed 4 partial glossectomies No chemo or radiation Biopsy on 2/2/10-Clear Surgery needed again...no later than April 2011 Loving life and just became a mother on 11/25/10 It's not what we CAN'T do..it's what we CAN do:)
| | | | Joined: Jan 2004 Posts: 64 Supporting Member (50+ posts) | Supporting Member (50+ posts) Joined: Jan 2004 Posts: 64 | Hi Teresa, I am sorry you are going through this. I dont know much about MTX aside from what I have read. It appears that some of the symptoms that Brian is experiencing may by caused by the drug, but should be reported to your physician. http://www.drugs.com/sfx/methotrexate-side-effects.html I dont think he should be working if he is experiencing the things he is. Also, I do know that 2 other posters here, Tom Rousell and suemarie's husband Neil had MTX, both palliative treatment. I dont think it is tolerated well. And I'm sorry if I missed something in your posts, but if he is this miserable with MTX, then why is he afraid of radiation?? I was 34 at diagnosis and went through radiation and chemo and tolerated it quite well, and I'm here to talk about it 7 years later. If he doesnt have radiation, he wont be so lucky. I agree with Suzanne that he may not be telling you the whole truth. Good luck to you and I hope you can convince him to seek further treatment.
SCC tonsil(left) with contralateral mets. Modified right neck disection August, 2002. 33 rads(62 gy)both sides of neck and 3 cycles cisplatin completed October 25, 2002. 34 yo at time of diagnosis
| | | | Joined: Aug 2009 Posts: 38 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Aug 2009 Posts: 38 | I do have a positive relationship with his family. However, his brother does know the situation and I feel like it is their place to go to his parents with this. Thanks for your input, though. It is greatly appreciated.
CG SCC of lower gum. DX 6/09, SURGERY 7/09, MTX Started 8/09. Single RX treatment 8/18/09
| | | | Joined: Sep 2006 Posts: 8,311 Senior Patient Advocate Patient Advocate (old timer, 2000 posts) | Senior Patient Advocate Patient Advocate (old timer, 2000 posts) Joined: Sep 2006 Posts: 8,311 | I'm sorry if I offend you but quite frankly this site is all about helping people that want to be helped and unfortunately you are the only one that wants our help and we can't help you other than some emotional support while you watch him die. It's frustrating to us as well when we know he probably could have been saved and we just don't understand how someone can act like him after this site has helped thousands that wanted to be helped.
Sorry and good luck.
David
Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
| | | | Joined: Apr 2006 Posts: 794 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Apr 2006 Posts: 794 | If I found that someone I loved had such a serious illness and had not trusted me enough to share the information with me so that I could either worry, pray, or help, I would be terribly insulted. I loved Charm's article, as I have had this philosophy for a long time: that to not allow others to help us when we need it is to reject a gift that they are trying to give us. It's a selfish act. You are suffering more than should be expected of you because of his irrational reaction to his illness. You are being expected to shoulder all of his care when there are others who could be supporting YOU and helping him.
Colleen--T-2N0M0 SCC dx'd 12/28/05...Hemi-maxillectomy, partial palatectomy, neck dissection 1/4/06....clear margins, neg. nodes....no radiation, no chemo....Cancer-free at 4 years!
| | | | Joined: Aug 2009 Posts: 38 Contributing Member (25+ posts) | OP Contributing Member (25+ posts) Joined: Aug 2009 Posts: 38 | Hello all. Can anyone tell me if they have had pain in the upper cheek bone- below the eye when laughing? I was so happy that I could finally make Brian laugh again sometimes and now every time that he does he grabs the side of his face. When I ask what is wrong he says he has a "crick in his cheek". He had a wisdom tooth cut out (that is how his cancer was found) on the upper right side. It was in the sinus cavity and that is where he seems to be hurting. Any suggestions what this is a sign or symptom of? We go from 75 mg MTX daily to a single 100 MG dose of Methotrexate once a week starting next week. That is the only update that I have on his "treatment" or lack of it. Teresa
CG SCC of lower gum. DX 6/09, SURGERY 7/09, MTX Started 8/09. Single RX treatment 8/18/09
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